HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848683Generated: October 26, 2026
5-Aminovaleric acid → 5-[[2-(Chloromethyl)-4-methyl-1-oxopentyl]amino]pentanoic acid
https://huagongshe.com/reaction/848683
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Aminovaleric acid | HCID 138 | — |
| Reactant | 2-(Chloromethyl)-4-methylvaleryl chloride | HCID 12769067 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 5-[[2-(Chloromethyl)-4-methyl-1-oxopentyl]amino]pentanoic acid | HCID 20563967 | — |
Reaction Steps
5-Aminovaleric acid (3.2 g) is dissolved in 15 ml of water containing 1.09 g of sodium hydroxide. This is cooled to 5° C. and 2-[chloromethyl]-4-methylvaleryl chloride in 30 ml of THF is added dropwise. The pH is maintained at 8-9 by the dropwise addition of 1.09 g sodium hydroxide in 20 ml of water as needed. After stirring for about 16 hours the reaction mixture is diluted with 30 ml of water and concentrated in vacuo to remove THF. The aqueous layer is washed with ether, and acidified with 10% hydrochloric acid. Product is extracted with ethyl acetate. The ethyl acetate is dried with magnesium sulfate, filtered and concentrated in vacuo to yield 4.3 g of product. Product is purified by chromatographing on 200 g of silica using as the solvent system 500 parts ether: 10 parts methanol: 5 parts acetic acid, yielding 2.0 g of material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04297275 |
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| Source dataset | uspto-grants-1981_10 |
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| ORD ID | ord-c8eb4d7ee286411b9faec544df72564a |
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| Source note | uspto-grants-1981_10 |
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